U.S. patent number 10,039,633 [Application Number 14/406,263] was granted by the patent office on 2018-08-07 for implantable prosthesis having acellular tissue attachments.
This patent grant is currently assigned to LifeCell Corporation. The grantee listed for this patent is LifeCell Corporation. Invention is credited to Matthew Amato, Heather Ansorge, Mark Hayzlett, Raymond Hull, Nimesh Kabaria, Lawrence Lapitan, Dennis Lee, Timothy Roock, Wenquan Sun, Michael Taenzer.
United States Patent |
10,039,633 |
Ansorge , et al. |
August 7, 2018 |
Implantable prosthesis having acellular tissue attachments
Abstract
A prosthesis comprising a tissue expander and one or more
samples of graft material, wherein the tissue expander is attached
to the one or more samples of graft material in a manner that
allows the tissue expander and the one or more samples of graft
material to be implanted in a patient as a unitary prosthesis; and
wherein tissue expander is attached to the one or more samples of
graft material in a manner that will allow the tissue expander and
the graft material to separate after a period of time following
implantation to allow removal of the tissue expander from an
implant sites while leaving the graft material within the implant
site, the prosthesis comprises a tissue expander having molded
grooves, slots, channels, or other shallow cavity spaces on a
surface, and wherein the graft material is within the grooves,
slots, channels, or other shallow cavity spaces, securing the graft
material to the tissue expander.
Inventors: |
Ansorge; Heather (New Hope,
PA), Lapitan; Lawrence (Jersey City, NJ), Hayzlett;
Mark (Flemington, NJ), Kabaria; Nimesh (Somerset,
NJ), Hull; Raymond (Hampton, NJ), Sun; Wenquan
(Warrington, PA), Taenzer; Michael (Hackettstown, NJ),
Amato; Matthew (Lawrenceville, NJ), Roock; Timothy
(Bordentown, NJ), Lee; Dennis (Scotch Plains, NJ) |
Applicant: |
Name |
City |
State |
Country |
Type |
LifeCell Corporation |
Branchburg |
NJ |
US |
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Assignee: |
LifeCell Corporation (Madison,
NJ)
|
Family
ID: |
48771701 |
Appl.
No.: |
14/406,263 |
Filed: |
June 18, 2013 |
PCT
Filed: |
June 18, 2013 |
PCT No.: |
PCT/US2013/046349 |
371(c)(1),(2),(4) Date: |
December 08, 2014 |
PCT
Pub. No.: |
WO2013/192197 |
PCT
Pub. Date: |
December 27, 2013 |
Prior Publication Data
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Document
Identifier |
Publication Date |
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US 20150150674 A1 |
Jun 4, 2015 |
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Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
Issue Date |
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61662840 |
Jun 21, 2012 |
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Current U.S.
Class: |
1/1 |
Current CPC
Class: |
A61B
90/02 (20160201); A61F 2/12 (20130101); A61F
2250/0071 (20130101); A61F 2220/005 (20130101); A61F
2220/0016 (20130101); A61F 2210/009 (20130101); A61F
2230/0004 (20130101); A61F 2230/0045 (20130101); A61F
2250/0003 (20130101); A61F 2230/0089 (20130101); A61F
2250/0051 (20130101); A61F 2210/0076 (20130101); A61F
2230/0093 (20130101); A61F 2220/0075 (20130101); A61F
2250/0031 (20130101); A61F 2220/0033 (20130101); A61F
2220/0091 (20130101); A61F 2220/0025 (20130101); A61F
2230/0086 (20130101); A61F 2250/0024 (20130101); A61F
2/0059 (20130101) |
Current International
Class: |
A61F
2/12 (20060101); A61B 90/00 (20160101); A61F
2/00 (20060101) |
References Cited
[Referenced By]
U.S. Patent Documents
Foreign Patent Documents
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102006029605 |
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Dec 2007 |
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DE |
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0338701 |
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Oct 1989 |
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EP |
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10-158906 |
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Jun 1998 |
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JP |
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WO-2003/084410 |
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Oct 2003 |
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WO |
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WO-2004/096098 |
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Nov 2004 |
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WO |
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WO-2006/115892 |
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Nov 2006 |
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WO |
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WO-2006/135998 |
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Dec 2006 |
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WO |
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WO-2007/004214 |
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Jan 2007 |
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WO |
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WO-2008/016919 |
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Feb 2008 |
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WO |
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WO-2008/121816 |
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Oct 2008 |
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WO |
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WO-2009/001293 |
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Dec 2008 |
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WO |
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WO-2009/065013 |
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May 2009 |
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WO |
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WO-2009/114052 |
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Sep 2009 |
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WO |
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WO-2013/106556 |
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Jul 2013 |
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WO |
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Other References
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Implant-related Problems": Plast. Reconstr. Surg.; 112(6):1692-1696
(2003). cited by applicant .
Bindingnavele et al.; "Use of acellular cadaveric dermis and tissue
expansion in postmastectomy breast reconstruction;" Journal of
Plastic, Reconstructive & Aesthetic Surgery; 60:1214-1218
(2007). cited by applicant .
Breuing et al.; "Immediate Bilateral Breast Reconstruction With
Implants and Inferolateral AlloDerm Slings"; Annals of Plastic
Surgery; 55(3):232-239 (2005). cited by applicant .
Breuing et al.; "Inferolateral AlloDerm Hammock for Implant
Coverage in Breast Reconstruction"; Annals of Plastic Surgery;
59(3):250-255 (2007). cited by applicant .
Colwell et al.; "Improving Shape and Symmetry in Mastopexy With
Autologous or Cadaveric Dermal Slings"; Annals of Plastic Surgery;
61(2):138-142 (2008). cited by applicant .
Darcy; "A Technique for Preparing Meshed Skin Grafts With Planned
Expansion Ratios"; British Journal of Plastic Surgery; 56(1):77-79
(2003). cited by applicant .
Duncan; "Correction of Implant Rippling Using Allograft Dermis";
Aesthetic Surgery Journal; 21(1):81-84 (2001). cited by applicant
.
Gamboa-Bobadilla; "Implant Breast Reconstruction Using Acellular
Dermal Matrix"; Annals of Plastic Surgery; 56(1):22-25 (2006).
cited by applicant .
Goes; "Periareolar Mammaplasty: Double Skin Technique with
Appliction of Polygractine 910 Mesh"; Rev. Soc. Bras. Cir. Plast.
Estet. Reconstr.; 7(1,2,3); pp. 1-6 (1992). cited by applicant
.
Goes; "Periareolar Mammaplasty: Double Skin Technique with
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applicant .
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Support"; Aesthetic Surgery Journal; 23:129-135 (Mar./Apr. 2003).
cited by applicant .
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Double Skin Technique"; Surgery of the Breast: Principles and Art;
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Skin Technique;" Operative Techniques in Plastic and Reconstructive
Surgery; 3(3):199-206 (Aug. 1996). cited by applicant .
Goes et al.; "The Application of Mesh Support in Periareolar Breast
Surgery: Clinical and Mammographic Evaluation;" Aesth. Plast.
Surg.; 28:268-274 (2004). cited by applicant .
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applicant .
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Surgery; 57(1):1-5 (2006). cited by applicant .
Topol et al.; "Immediate Single-Stage Breast Reconstruction Using
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applicant.
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Primary Examiner: Iwamaye; Andrew
Attorney, Agent or Firm: McCarter & English, LLP
Parent Case Text
This application is a 35 U.S.C. .sctn. 371 national stage filing of
International Application No. PCT/US2013/046349, filed on Jun. 18,
2013, which claims the benefit of priority under 35 U.S.C. .sctn.
119 to U.S. Provisional Application No. 61/662,840, filed on Jun.
21, 2012, the content of each of which is incorporated herein by
reference in its entirety.
Claims
What is claimed is:
1. A prosthesis comprising: a tissue expander comprising molded
grooves, slots, or channels on a surface of the tissue expander;
and one or more samples of graft material comprising adipose tissue
matrix releasably coupleable to the tissue expander in a manner
that allows the tissue expander and the adipose tissue matrix to be
implanted in a patient as a unitary prosthesis, wherein the adipose
tissue matrix further comprises shaped protrusions that conform to
the inner surfaces of the grooves, slots, or channels on the
surface of the tissue expander to releasably couple the adipose
tissue matrix to the tissue expander, and wherein the adipose
tissue matrix is configured to release from the tissue expander as
the tissue expander is enlarged after implantation.
2. The prosthesis of claim 1, wherein the adipose tissue matrix
comprises an acellular adipose tissue matrix.
3. The prosthesis of claim 2, wherein the adipose acellular tissue
matrix has been treated to produce a three-dimensional porous or
sponge-like material.
4. The prosthesis of claim 1, wherein the adipose tissue matrix is
configured to release from the tissue expander as a frictional
force holding the adipose tissue matrix in place lessens after
implantation.
5. The prosthesis of claim 1, wherein the adipose tissue matrix is
configured to release from the molded slots, grooves, or channels
as the tissue expander is filled after implantation, thereby
stretching the edges of the molded slots, grooves, or channels and
removing a frictional force coupling the adipose tissue matrix to
the tissue expander.
6. The prosthesis of claim 1, wherein the shaped protrusions are
configured to release from the molded slots, grooves, or channels
as the tissue expander or the adipose tissue matrix deforms
following implantation thereby lessening a frictional force
coupling the adipose tissue matrix to the tissue expander.
Description
Disclosed herein are implantable prostheses, such as breast
implants and tissue expanders, for use in various surgical
procedures.
Implantable prostheses, such as breast implants and tissue
expanders, are used in a wide range of surgical procedures. For
example, the prostheses can be used for breast augmentation,
reconstruction, and/or revision. But, even though the implants and
tissue expanders used in these surgical procedures are
biocompatible and non-reactive, post-surgical complications can
still result from their use, such as capsular contracture, scar
formation, implant displacement, rippling, and palpability of
implants. Research has focused on surgical techniques and modified
implant characteristics, which may result in reduced incidence of
complications. One approach that surgeons use to improve outcomes,
reduce the risk of complications, and/or provide improved revisions
is to use graft materials, such as acellular dermal tissue matrices
like ALLODERM.RTM. or STRATTICE.TM. (LIFECELL CORPORATION,
Branchburg, N.J.), along with the tissue expanders or breast
implants.
The current standard of care during surgical breast procedures
involves separately attaching a graft material to a patient and
then placing a prosthesis in the patient. In one procedure the
surgeon first attaches the graft material to the infra mammary fold
(IMF) and the pectoralis major muscle in order to create a
submuscular pocket or flap. Next, the surgeon places the breast
implant or tissue expander inside the pocket. The process of
attaching the graft material to the native tissue can require a
substantial amount of time and involve the use of sutures or other
devices to anchor the graft material to the native tissue. The
current process can also lead to inconsistent results, as
inexperienced surgeons may not use graft materials of optimal
shape, or may incorrectly position the implant or tissue expander
relative to the graft material.
Accordingly, there is a need for improved prostheses comprising
tissue expanders, methods of making these prostheses, and methods
of treatment using such prostheses.
In various embodiments, an implantable prosthesis is disclosed
herein, comprising a tissue expander and one or more samples of
graft material, wherein the tissue expander is attached to the one
or more samples of graft material in a manner that allows the
tissue expander and the one or more samples of graft material to be
implanted in a patient as a unitary prosthesis, and wherein the
implant or tissue expander is attached to the one or more samples
of graft material in a manner that will allow the tissue expander
and the graft material to be easily separated naturally or through
surgical intervention after a period of time following
implantation. In some embodiments, the prosthesis comprises molded
grooves, slots, channels or other shallow cavity spaces that secure
the graft material to the tissue expander. In certain embodiments,
the prosthesis comprises a biocompatible flap or pocket on the
surface of the tissue expander that secures the graft material to
the tissue expander.
In some embodiments, the prosthesis comprises one or more fixation
tacks comprising one or more thin strands of biocompatible material
and one or more barbs that secure the graft material to the tissue
expander. In some embodiments, the prosthesis comprises one or more
zip ties that secure the graft material to the tissue expander. In
some embodiments, the one or more samples of graft material
comprise one or more holes, slits, or apertures through which the
one or more fixation tacks or zip ties are passed to secure the
graft material to the tissue expander.
In certain embodiments, the prosthesis comprises a belt that
secures the graft material to the tissue expander. In some
embodiments, the belt comprises slots, and the graft material is
shaped to provide tabs or other shapes that will fit within the
slots on the belt, thereby securing the graft material to the
belt.
In some embodiments, the prosthesis comprises attachment points,
wherein the attachment points comprise a dissolvable hard material,
are attached to an exterior surface of the tissue expander or
underneath the exterior surface of the tissue expander, and are in
the form of dissolvable tabs, clips, balls, or buttons. In some
embodiments, the one or more samples of graft material comprise one
or more holes, slits, or apertures through which the attachment
points are passed to secure the graft material to the tissue
expander. In some embodiments, the attachment points dissolve or
otherwise detach after a period of time following implantation,
thereby releasing the graft material.
In certain embodiments, a prosthesis further comprises one or more
magnets that secure the graft material to the tissue expander. In
some embodiments, the prosthesis also comprises a biocompatible
flap and two or more magnets, wherein at least one magnet is
secured to a surface of the tissue expander and at least one magnet
is secured to the flap on the tissue expander, and wherein the
graft material is secured between the two magnets.
In various embodiments, the graft material comprises an acellular
tissue matrix. For example, the acellular tissue matrix can
comprise an adipose acellular tissue matrix that has been treated
to produce a three-dimensional porous or sponge-like material.
In various embodiments, a method of making an implantable
prosthesis is disclosed, comprising attaching one or more samples
of graft material to a tissue expander comprising at least one of:
one or more molded grooves, slots, channels or other shallow cavity
spaces; a flap or pocket; one or more fixation tacks; one or more
zip ties; a belt; one or more attachment points; or one or more
magnets. In some embodiments, the graft material is secured to the
tissue expander by interacting with the one or more molded grooves,
slots, channels or other shallow cavity spaces; flap or pocket;
belt; one or more fixation tacks; one or more zip ties; one or more
attachment points; or one or more magnets. In some embodiments,
after attaching the graft material to the shell of the tissue
expander, the prosthesis is heat cured. In some embodiments, the
prosthesis is heat cured at a temperature of about 30.degree. C. or
less, or at a temperature of between about 70.degree. C. and
120.degree. C.
Furthermore, in various embodiments, methods of treatment using the
disclosed prostheses are provided herein, comprising implanting a
prosthesis into a tissue and then removing the tissue expander
after a predetermined length of time while leaving the one or more
samples of graft material at the implant site. In some embodiments,
the tissue expander separates from the graft material over time
following implantation without requiring surgical intervention. In
other embodiments, the tissue expander is manually separated from
the graft material prior to removal of the tissue expander. In
certain embodiments, a prosthesis as disclosed herein is implanted
as part of a breast augmentation procedure.
BRIEF DESCRIPTION OF THE DRAWINGS
FIG. 1A illustrates a portion of a prosthesis, according to certain
embodiments of the disclosure, comprising a tissue expander having
a grooved surface and a graft material shaped to conform to the
grooves. FIG. 1B shows the graft material secured to the grooves on
the tissue expander.
FIG. 2 illustrates a portion of a prosthesis, according to certain
embodiments, comprising a tissue expander having a polymeric flap,
wherein the flap serves to secure a graft material to the surface
of the prosthesis.
FIG. 3 illustrates a portion of a prosthesis, according to certain
embodiments, comprising a tissue expander having two thin polymeric
cords that can be passed through holes in a graft material and
attached to the surface of the tissue expander using fixation tacks
provided at the ends of the thin polymeric cords.
FIG. 4 illustrates a portion of a prosthesis, according to certain
embodiments, comprising a tissue expander having two zip ties that
can be passed through holes in a graft material and thereby secure
the graft material to the tissue expander.
FIG. 5A illustrates a portion of a prosthesis, according to certain
embodiments, comprising a tissue expander having a polymeric belt
used to secure a graft material to the tissue expander. FIG. 5B
illustrates a portion of a prosthesis, according to certain
embodiments, comprising a tissue expander having a polymeric belt
comprising slots used to secure a graft material to the tissue
expander. FIG. 5C illustrates a portion of a graft material,
according to certain embodiments, shaped to have components that
will fit into the slots in the belt shown in FIG. 5B.
FIG. 6 illustrates a portion of a prosthesis, according to certain
embodiments, comprising a tissue expander having a flap of
biocompatible material and two magnets used to secure the open end
of the flap to the tissue expander.
FIG. 7A-C illustrates portions of prostheses, according to certain
embodiments, comprising tissue expanders having examples of three
different types of attachment points for use in securing a graft
material to the tissue expander. FIG. 7D illustrates a portion of a
graft material, according to certain embodiments, having holes for
use in securing the graft material to the tissue expanders shown in
FIG. 7A-C.
DESCRIPTION OF CERTAIN EXEMPLARY EMBODIMENTS
Reference will now be made in detail to certain exemplary
embodiments of the invention, certain examples of which are
illustrated in the accompanying drawings.
In this application, the use of the singular includes the plural
unless specifically stated otherwise. In this application, the use
of "or" means "and/or" unless stated otherwise. Furthermore, the
use of the term "including," as well as other forms, such as
"includes" and "included," is not limiting. Any range described
herein will be understood to include the endpoints and all values
between the endpoints. Also, terms such as "element" or "component"
encompass both elements and components comprising one subunit and
elements and components that comprise more than one subunit, unless
specifically stated otherwise. Also, the use of the term "portion"
may include part of a moiety or the entire moiety.
The section headings used herein are for organizational purposes
only and are not to be construed as limiting the subject matter
described. All documents, or portions of documents, cited in this
application, including but not limited to patents, patent
applications, articles, books, and treatises, are hereby expressly
incorporated by reference in their entirety for any purpose.
The term "graft material," as used herein, generally refers to a
biocompatible material, or a combination of biocompatible
materials, such as, for example, one or more samples of tissue,
processed tissue, partially or completely decellularized tissue,
and/or synthetic material that can be attached to a prosthesis,
inserted into an implant site, and promote the migration and/or
proliferation of native cells within the graft material.
The terms "breast implant" and "implant," as used herein, generally
refer to medical devices that are implanted either under or within
breast tissue or under the chest muscle for breast augmentation or
reconstruction. Such implants can include saline filled or silicone
gel implants, or other implants that provide volume for breast
augmentation. The terms "breast tissue expander," "tissue
expander," and "expander," as used herein, generally refer to
devices that are implanted under or within breast or other tissue
or muscle, and which are expanded over time to stretch breast or
other tissue and skin. The tissue expander can be made from any
biocompatible and/or non-reactive material commonly used in
implantable medical devices such as standard tissue expanders or
breast implants. Unless otherwise indicated, different tissue
expanders can be used interchangeably with the different graft
materials and methods disclosed herein. Furthermore, the term
"prosthesis" will be understood to include any implantable device
disclosed herein that comprises a tissue expander component and one
or more samples of graft material.
The term "resorbable biocompatible polymer," as used herein, refers
to a polymer that can be dissolved or otherwise absorbed by the
body over time following implantation and which does not elicit a
substantial immune or inflammatory response following implantation.
A substantial immune or inflammatory response includes any response
that prevents or hinders the migration of native cells into the
extracellular matrix of the graft material or prevents the partial
or complete repopulation of the graft material with native cells.
For example, the resorbable polymer can comprise aliphatic
polyester polymers and copolymers and blends thereof, polymers of
lactide or galactide or copolymers thereof, polysaccharides such as
cellulose, oxidized polysaccharides, or other absorbable polymers.
As used herein, the terms "native cells" and "native tissue" mean
the cells and tissue present in the recipient tissue/organ prior to
the implantation of a prosthesis, or the cells or tissue produced
by the host animal after implantation
The present disclosure relates to prostheses, methods of making
prostheses, and methods of treatment using the prostheses. In
various embodiments, the prostheses disclosed herein can be used
with any surgical procedure where tissue expansion is desirable
(e.g., to stretch tissue harvested for use in autologous skin
grafts). As such, the implantable prostheses and methods discussed
herein may be suitable for a wide range of surgical applications.
In some embodiments, the prostheses and methods discussed herein
may be suitable for various types of surgical breast procedures,
such as, for example, aesthetic surgery associated with mastectomy
or lumpectomy, breast reconstruction, breast augmentation, breast
enhancement, mastopexy, and/or revisionary breast surgeries.
According to certain embodiments, a prosthesis is disclosed. The
prosthesis can comprise a tissue expander and one or more samples
of graft material, wherein the tissue expander is attached to the
one or more samples of graft material in a manner that allows the
tissue expander and the one or more samples of graft material to be
implanted in a patient as a unitary prosthesis; and wherein the
implant or tissue expander is attached to the one or more samples
of graft material in a manner that will allow the tissue expander
and the graft material to be easily separated after a period of
time following implantation. The tissue expander can be made from
any biocompatible and/or non-reactive material commonly used in
implantable medical devices such as standard tissue expanders or
breast implants.
In certain embodiments, the structure of the tissue expander, along
with its attachment to a graft material such as an acellular tissue
matrix, allows the tissue expander to be enlarged and subsequently
removed after a certain period of time, without removing the graft
material. Accordingly, the devices and methods of the present
disclosure can be beneficial for reconstruction procedures that
require removal of tissue expanders but where retention of a graft
material would be desirous.
By providing a tissue expander and one or more samples of graft
material as a unitary prosthesis, the implantable prostheses of the
present disclosure can, in some embodiments, shorten procedure
time, reduce the number of surgical sutures, staples and/or other
attachment devices needed to secure the prostheses, and reduce the
associated costs of surgery. In certain embodiments, the
implantable prostheses can also improve surgical outcomes and
improve consistency of results. In some embodiments, the
implantable prostheses reduce the incidence of extrusion and/or
capsular contraction, block or reduce inflammatory responses,
and/or result in shorter expansion times.
In some embodiments, the tissue expanders can be implanted as
unitary prostheses. In some embodiments, the implantable prostheses
of the present disclosure can be constructed such that the tissue
expander can easily separate from the graft material after
implantation. In various embodiments, the graft material is
attached to the tissue expander in such a way that the two will
separate before the tissue expander is removed. In some
embodiments, the tissue expander is designed to separate from the
graft material after a period of time. In certain embodiments, the
graft material is attached to the tissue expander in such a way
that the graft material and tissue expander will separate without
requiring surgical intervention. In other embodiments, the graft
material is attached to the tissue expander in such a way that the
two can be easily separated when the tissue expander is surgically
removed, leaving the graft material at the implant site.
According to certain embodiments, a prosthesis is disclosed that
comprises a tissue expander and one or more samples of graft
material sized and/or shaped to conform to a portion of a surface
of the tissue expander, wherein the one or more samples of graft
material is attached to the tissue expander in such a way as to
temporarily secure the graft material in place but to release the
graft material from the tissue expander over time following
implantation.
For example, in some embodiments, a tissue expander may comprise
molded grooves, slots, channels or other shallow cavity spaces on
the surface of the expander. For instance, FIG. 1A illustrates a
portion of a tissue expander having a surface 103 containing
grooves 101. Graft material 104, optionally containing shaped
components 102 that conform to the grooves 101 or other cavity
spaces, can be placed within the cavity spaces in the tissue
expander. In some embodiments, the graft material 104 is initially
held in place by the edges of the cavity spaces in the tissue
expander (FIG. 1B), which press against all or some of the graft
material 104 and provide a frictional force to prevent the graft
material 104 from migrating away from the expander. Over time, the
graft material 104 can separate from the tissue expander. For
example, the graft material 104 may naturally migrate away from the
expander as the frictional force holding it in place lessens after
implantation (e.g., due to the aqueous environment, due to the
deformation of the expander or the graft material following
implantation, and/or due to the natural flexibility of the grooves,
slots, channels or other shallow cavity spaces). Alternatively, in
some embodiments the graft material 104 may be released from the
cavity spaces as the tissue expander is filled after implantation,
thereby stretching the edges of the cavity space and removing the
frictional force securing the graft material 104 to the
expander.
In another example, a graft material can be secured to a tissue
expander by a flap or pocket of biocompatible material on the
surface of the tissue expander. In some embodiments, the flap or
pocket is secured at one end but able to slide relative to the
underlying surface of the tissue expander. For example, FIG. 2
illustrates a portion of a prosthesis 201 comprising a tissue
expander 202 having a polymeric flap or pocket 204, wherein the
flap or pocket 204 serves to secure a graft material 203 to the
surface of the tissue expander 202. The flap or pocket 204 can
comprise a biocompatible material (e.g., silicone). The graft
material 203 can be placed in the flap or pocket 204, temporarily
securing the graft material 203 to the expander 202. As the tissue
expander 202 is filled, the flap or pocket 204 is retracted,
releasing the graft material 203.
In yet another example, a graft material can be secured to a tissue
expander using fixation tacks. For example, a tissue expander can
comprise one or more thin cords or strands of biocompatible
material (e.g., silicone). In some embodiments, the cords can have
a branched structure, such as a T-tack structure. In certain
embodiments, the ends of the cords can comprise tacks or other
textured surfaces that can engage the surface of a tissue expander
and/or a graft material. In some embodiments, a graft material
comprising at least one hole is secured to the tissue expander by
passing the one or more cords or strands through the at least one
hole in the graft material. In certain embodiments, the tacks or
textured surface on the end of the cord or strand is placed in
contact with the tissue expander or graft material after being
passed through the one or more holes on the graft material,
anchoring the graft material to the expander. In some embodiments,
the graft material comprises at least two holes, and the cords or
strands are threaded through both holes, thereby anchoring the
graft to the underlying expander. In various embodiments, filling
the tissue expander exerts tension on the cords or strands, causing
the tacks or other textured surfaces to release, thereby freeing
the graft material from the tissue expander. In other embodiments,
the cords or strands comprise a resorbable polymer (e.g., aliphatic
polyester polymers, copolymers, blends thereof, polymers of
lactide, galactide, or copolymers thereof, polysaccharides such as
cellulose, and oxidized polysaccharides, or other absorbable
polymers) that dissolves over time following implantation, thereby
releasing the graft material. For example, FIG. 3 illustrates a
portion of a prosthesis 301 comprising a tissue expander 302 having
two thin polymeric cords 304 that pass through holes 305 in a graft
material 306 and attach to the surface of the tissue expander 302
using fixation tacks 303.
In still another example, a graft material can be secured to a
tissue expander using zip ties. For example, a tissue expander
comprising one or more attached zip ties can be prepared. The zip
ties can comprise a biocompatible material (e.g., silicone). In
some embodiments, the zip ties are passed through one or more holes
in a graft material and then passed through the locking point in
the zip tie, securing the graft material to the tissue expander. In
some embodiments, the zip ties are manually released by the surgeon
prior to surgical removal of the tissue expander. In another
embodiment, the zip ties are prepared from a resorbable,
biocompatible material that dissolves over time after exposure to
the aqueous implant environment, thereby releasing the graft
material. In certain embodiments, the resorbable polymer can
comprise aliphatic polyester polymers, copolymers, blends thereof,
polymers of lactide, galactide, or copolymers thereof,
polysaccharides such as cellulose, and oxidized polysaccharides, or
other absorbable polymers). For example, FIG. 4 illustrates a
portion of a prosthesis 401 comprising a tissue expander 402 having
two zip ties 403 that pass through holes 404 in a graft material
405 and secure the graft material 405 to the tissue expander
402.
In another example, a tissue expander can comprise a belt used to
secure a graft material. For example, FIG. 5A illustrates a portion
of a prosthesis 501 comprising a tissue expander 502 having a
polymeric belt 503 used to secure a graft material to the tissue
expander 502. In various embodiments, the belt 503 may comprise a
biocompatible material (e.g., silicone). In some embodiments, the
graft material can be inserted under the belt 503, securing the
graft to the expander 502. In certain embodiments, the belt can
comprise slots, and the graft material can be shaped to provide
tabs or other shapes that will fit within the slots on the belt,
thereby securing the graft material to the belt. For example, FIG.
5B illustrates a portion of a prosthesis 501 comprising a tissue
expander 502 having a polymeric belt 503 comprising slots 504 used
to secure a graft material to the tissue expander 502. In some
embodiments, a graft material, such as the graft material 506 shown
in FIG. 5C, is shaped to have components 505 that will fit into the
slots 504 in the belt 503, thereby securing the graft material 506
to the tissue expander 502.
In some embodiments, as the tissue expander is filled, the belt
that secures the graft to the expander is stretched, reducing the
tension applied by the belt on the graft material, and thereby
releasing the graft material from the tissue expander. In other
embodiments, the graft material is manually released from the belt
by the surgeon when the tissue expander is removed. In other
embodiments, the belt comprises a resorbable polymer (e.g.,
aliphatic polyester polymers, copolymers, blends thereof, polymers
of lactide, galactide, or copolymers thereof, polysaccharides such
as cellulose, and oxidized polysaccharides, or other absorbable
polymers) that dissolves over time following implantation, thereby
releasing the graft material.
In various embodiments, a tissue expander can comprise attachment
points (e.g., clips, balls, buttons or tabs) on at least a portion
of the outer surface. For example, FIG. 7A-C illustrates portions
of tissue expanders having three different types of attachment
points 701, 702, and 703 for use in securing a graft material to
the tissue expander. The attachment points 701-703 can be used to
secure the graft material to the expander, for example by folding
over the edges of the graft material, or by pushing the attachment
points 701-703 through holes, slits, or other perforations placed
in the graft material, thereby securing the graft material in
place. For example, FIG. 7D illustrates a portion of a graft
material 704 having holes 705 through which the attachment points
701-703 can be passed to secure the graft material 704 to the
tissue expander. The attachment points 701-703 can have any shapes
suitable for securing a graft material, for example balls,
cylinders, cylinders with widened heads, button, curved shapes,
etc. Over time, the attachment points 701-703 are designed to
dissolve, separate, detach, or otherwise release the graft material
704 from the tissue expander.
For example, in certain embodiments a hard material can be placed
underneath the outer membrane of the tissue expander and press out
through the membrane to create the attachment points. For example,
a hard material in the shape of tabs, clips, balls, buttons, or
other desired shapes can be affixed along the inner surface of the
expander and bulge out through the membrane to create attachment
points for the graft material. The hard material can be used to
secure the graft material to the expander, for example by folding
over the edges of the graft material, or by pushing through holes,
slits, or other perforations placed in the graft material, thereby
securing the graft material in place. In some embodiments, the hard
material comprises a material that is soluble in aqueous solution.
Over time, the saline or other aqueous solution in the tissue
expander can dissolve the hard material, thereby releasing the
graft material. Examples of suitable hard materials include, but
are not limited to, poly-caprolactone, polylactic acid,
polygalacturonic acid, polymer polyglycolic-lactic acid,
polyhydroxyalkanoates, polydioxanone, or any other similar polymers
or biological materials known to degrade in vivo.
In another example, the attachment points can comprise a hard
material attached to the external surface of a tissue expander. In
some embodiments, the attachment points comprise tabs, clips,
balls, buttons, or other desired shapes that secure the graft
material to the expander, for example by folding over the edges of
the graft material, or by pushing through holes, slits, or other
perforations placed in the graft material, thereby securing the
graft material in place. In some embodiments, the attachment points
are designed to release when exposed to force as the tissue
expander is filled. For example, filling the tissue expander can
lift or stretch the tabs that hold a graft material against a
tissue expander, bending the tabs away from the graft material and
releasing the graft material from the expander. Similarly, in
another example, filling the tissue expander can stretch the graft
material secured to it, thereby transmitting a torsional force to
the attachment points (e.g., the tabs, clips, balls, buttons, or
other shapes) as the graft material pulls on them, resulting in the
deformation or detachment of the attachment points and release of
the graft material. In other embodiments, the attachment points may
comprise a resorbable, biocompatible material that dissolves over
time when exposed to the aqueous environment of the implant site,
thereby releasing the graft material. For example, the resorbable
material can comprise aliphatic polyester polymers, copolymers,
blends thereof, polymers of lactide, galactide, or copolymers
thereof, polysaccharides such as cellulose, and oxidized
polysaccharides, or other absorbable polymers that dissolve over
time following implantation, thereby releasing the graft
material.
In various embodiments, a graft material can be secured to a tissue
expander using one or more magnets. For example, FIG. 6 illustrates
a portion of a prosthesis 601 comprising a tissue expander 602
having a flap 604 of biocompatible material and two magnets 603,
with one portion of the magnet 603 secured to the inner surface of
the tissue expander 602 and the other portion of the magnet 603
secured to the flap 604 of the tissue expander 602. In some
embodiments, a graft material can be placed over the tissue
expander 602 or over a portion of the tissue expander 602
comprising the at least one magnet 603. The flap 604 comprising at
least one magnet 603 can be folded down over the graft material to
interact with the magnet 603 on the inner surface of the tissue
expander 602, thereby securing the graft material between the flap
604 and the tissue expander 602. In some embodiments the one or
more magnets and the flap comprise biocompatible materials.
According to certain embodiments, a method of making a prosthesis
is provided. The method can comprise providing a tissue expander
and one or more samples of graft material that is sized and/or
shaped to conform to at least a portion of a surface of the tissue
expander, and attaching the one or more samples of graft material
to the tissue expander using one of the attachment methods
described above. The tissue expanders disclosed herein can be
formed from a variety of suitable materials. For example, the shell
of an expander may be produced from a material that is designed to
prevent tissue ingrowth and/or adhesion, and which can expand when
placed under force during filling. For example, in some
embodiments, a tissue expander can be formed from a material that
provides a smooth shell, such as silicone. In other embodiments, a
tissue expander is made from a material that provides a desired
surface texture, or the tissue expander is molded during formation
to provide a desired surface texture.
In some embodiments, the tissue expander can be attached to the one
or more samples of graft material in a medical setting or in the
operating room just prior to implanting a prosthesis in a patient.
In some embodiments, the tissue expander can be attached to the one
or more samples of graft material prior to a surgery. In some
embodiments, the tissue expander can be attached to the one or more
samples of graft material prior to the surgery, so that the
implantable prosthesis can be sold as a ready-to-use, off the shelf
prosthesis. In some embodiments, a package or kit can comprise a
prosthesis, comprising the tissue expander pre-attached to the one
or more graft materials, or provided as two separate components
within the package or kit. In some embodiments, the prosthesis in
the kit is packaged under aseptic or sterile conditions. In certain
embodiments, the kit can further comprise instructions for using
the tissue expander.
In various embodiments, the graft materials are further secured to
the tissue expander using biodegradable sutures, biocompatible
adhesives, biocompatible glues, and/or any means of attachment
known by one of skill in the art.
According to certain embodiments, methods of making a prosthesis
are disclosed, comprising preparing a tissue expander, providing
one or more samples of graft material sized and shaped to conform
to at least a portion of a surface of a tissue expander, attaching
the graft material to the shell of the tissue expander using any of
the attachment methods described above to form a prosthesis, and
optionally curing and/or irradiating the prosthesis.
In some embodiments the graft material comprises an acellular
tissue matrix. In some embodiments the graft material comprises an
acellular tissue matrix that has been treated to produce a
three-dimensional porous, or sponge-like material.
In some embodiments the shell of the tissue expander and the
acellular tissue matrix are cured such that the curing temperature
does not reach a temperature greater than 30.degree. C. In some
embodiments the shell of the tissue expander and the acellular
tissue matrix are cured such that the curing temperature does not
exceed 25.degree. C. In some embodiments the shell of the tissue
expander and the extracellular tissue matrix are cured such that
the curing temperature is between about 70.degree. C. and
120.degree. C., or between about 80.degree. C. and 110.degree. C.,
or about 100.degree. C. In some embodiments lower or higher
temperatures could be used as long as melting of the matrix
proteins does not occur.
The graft materials and tissue expanders discussed herein can
include one or more biocompatible materials. The biocompatible
material can comprise any suitable synthetic or biologic material,
such as, for example, medical grade silicone, autologous or
cadaveric tissue, and/or biomatrices, such as, for example, an
acellular tissue matrix ("ATM"). In some embodiments, the
biocompatible material may be a flat sheet or sheet-like in form. A
biocompatible material may be a single layer or may be
multi-layered. In some embodiments, a biocompatible material may be
a material that facilitates cell migration, repopulation, and/or
revascularization. For example, in certain embodiments, a graft
material can include an acellular tissue matrix ("ATM").
As used herein, ATM refers to a tissue-derived biomatrix structure
that can be made from any of a wide range of collagen-containing
tissues by removing all, or substantially all, viable cells and all
detectable subcellular components and/or debris generated by
killing cells. As used herein, an ATM lacking "substantially all
viable cells" is an ATM in which the concentration of viable cells
is less than 1% (e.g., less than: 0.1%; 0.01%; 0.001%; 0.0001%;
0.00001%; or 0.000001%; or any percentage in between) of the viable
cells in the tissue or organ from which the ATM was derived.
For a description of exemplary ATMs that are suitable for use in
the present disclosure, as well as methods of making those ATMs,
see co-pending U.S. application Ser. No. 12/506,839 (published as
US 2011/0022171) at paragraphs 41-73 and U.S. Provisional
Application No. 61/491,787 at paragraphs 23-38 and 42-56, which are
incorporated herein by reference in their entirety. Additionally,
as non-limiting examples of methods of producing ATMs, mention is
made of the methods described in U.S. Pat. Nos. 4,865,871;
5,366,616; and 6,933,326, and U.S. Patent Application Publication
Nos. US2003/0035843 A1, and US 2005/0028228 A1, all of which are
incorporated herein by reference in their entirety.
In some embodiments, the graft material can comprise STRATTICE.TM.,
a porcine dermal tissue produced by Lifecell Corporation
(Branchburg, N.J.). In some embodiments, the graft material can
comprise ALLODERM.RTM., an ATM produced from human dermis by
LifeCell Corporation (Branchburg, N.J.).
In some embodiments, the graft material comprises an adipose tissue
matrix. In some embodiments the graft material comprises an adipose
tissue matrix that has been treated to produce a three-dimensional
porous, or sponge-like material. For a description of adipose
tissue matrices that are suitable for use in the present
disclosure, as well as methods of making adipose tissue matrices,
see U.S. Provisional Application No. 61/491,787 at paragraphs 23-38
and 42-56, which is incorporated by reference in its entirety.
Briefly, the process generally includes obtaining adipose tissue,
mechanically processing the adipose tissue to produce small pieces,
further processing the tissue to remove substantially all cellular
material and/or lipids from the tissue, resuspending the tissue in
a solution to form a porous matrix or sponge, and optionally
cross-linking the tissue to stabilize a desired three-dimensional
structure.
In certain embodiments, ready-to-use, off-the-shelf materials that
are designed or further processed to conform to tissue expanders of
various specifications can be used as graft materials. For a
description of methods of making graft materials that are suitable
for use in the present disclosure, see co-pending U.S. application
Ser. No. 12/506,839 (published as US 2011/0022171). The disclosure
of U.S. application Ser. No. 12/506,839 is incorporated herein by
reference in its entirety.
In certain embodiments, methods of treatment are provided,
comprising providing any of the prostheses described above and
implanting the prosthesis into a site on a patient where a
prosthesis is required (e.g., as part of a breast augmentation
procedure). In certain embodiments, a prosthesis is used following
a breast cancer therapy (e.g., to expand remaining native skin to
receive a breast implant following a mastectomy). In other
embodiments, a prosthesis is used as part of a cosmetic procedure
(e.g., as part of a breast alteration procedure).
Other embodiments of the invention will be apparent to those
skilled in the art from consideration of the specification and
practice of the invention disclosed herein. It is intended that the
specification and examples be considered as exemplary only, with a
true scope and spirit of the invention being indicated by the
following claims.
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